WO2014170537A1 - A method and a device for cross-talk correction of measured intensities - Google Patents

A method and a device for cross-talk correction of measured intensities Download PDF

Info

Publication number
WO2014170537A1
WO2014170537A1 PCT/FI2014/050246 FI2014050246W WO2014170537A1 WO 2014170537 A1 WO2014170537 A1 WO 2014170537A1 FI 2014050246 W FI2014050246 W FI 2014050246W WO 2014170537 A1 WO2014170537 A1 WO 2014170537A1
Authority
WO
WIPO (PCT)
Prior art keywords
probe
detection wavelength
cross
talk
wavelength bands
Prior art date
Application number
PCT/FI2014/050246
Other languages
English (en)
French (fr)
Inventor
Ville Laitala
Raimo Harju
Original Assignee
Wallac Oy
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wallac Oy filed Critical Wallac Oy
Priority to US14/784,768 priority Critical patent/US9736555B2/en
Priority to BR112015025832-8A priority patent/BR112015025832B1/pt
Priority to CN201480033905.7A priority patent/CN105324493B/zh
Priority to EP14721911.7A priority patent/EP2986737A1/en
Publication of WO2014170537A1 publication Critical patent/WO2014170537A1/en

Links

Classifications

    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04QSELECTING
    • H04Q11/00Selecting arrangements for multiplex systems
    • H04Q11/0001Selecting arrangements for multiplex systems using optical switching
    • H04Q11/0005Switch and router aspects
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6816Hybridisation assays characterised by the detection means
    • C12Q1/6818Hybridisation assays characterised by the detection means involving interaction of two or more labels, e.g. resonant energy transfer
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/27Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands using photo-electric detection ; circuits for computing concentration
    • G01N21/274Calibration, base line adjustment, drift correction
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • G01N21/6452Individual samples arranged in a regular 2D-array, e.g. multiwell plates
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04QSELECTING
    • H04Q11/00Selecting arrangements for multiplex systems
    • H04Q11/0001Selecting arrangements for multiplex systems using optical switching
    • H04Q11/0003Details
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2537/00Reactions characterised by the reaction format or use of a specific feature
    • C12Q2537/10Reactions characterised by the reaction format or use of a specific feature the purpose or use of
    • C12Q2537/101Homogeneous assay format, e.g. one pot reaction
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N2021/6417Spectrofluorimetric devices
    • G01N2021/6421Measuring at two or more wavelengths
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6428Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
    • G01N2021/6439Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks
    • G01N2021/6441Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks with two or more labels
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04QSELECTING
    • H04Q11/00Selecting arrangements for multiplex systems
    • H04Q11/0001Selecting arrangements for multiplex systems using optical switching
    • H04Q11/0005Switch and router aspects
    • H04Q2011/0037Operation
    • H04Q2011/0049Crosstalk reduction; Noise; Power budget

Definitions

  • the disclosure of this document relates to a method for cross-talk correction of in- tensities measured on two or more detection wavelength bands from a sample. Furthermore, the disclosure relates to a device and to a computer program for cross-talk correction of intensities measured on two or more detection wavelength bands from a sample. Furthermore, the disclosure relates to a measurement instrument provided with cross-talk correction. Background
  • a widely used principle in multianalyte assays is to use labeled analyte-specific tracer molecules where concentrations of analytes in a sample can be detected on the basis of changes taking place in fluorescence-based emission signals that may be dependent on one or more excitation wavelengths used.
  • fluorescence-based emission signals related to different analytes occur on non- overlapping detection wavelength bands and therefore the emission signals can be separated from each other with straightforward optical filtering.
  • one or more of the spectra of the fluorescence-based emission signals related to different analytes is/are so wide and spectrally overlapping that it is not possible to select such detection wavelength bands that all emission signals measured on these detection wavelength bands would be free from cross-talk.
  • a simple principle for cross-talk correction is applicable in two-analyte assays where intensity of one of the emission signals can be measured cross-talk free using a suitable temporal detection window and/or a suitable detection wavelength band.
  • the measured intensity of the other emission signal is corrected using the measured intensity of the first emission signal and an empirical cross-talk parameter which indicates the relation between the intensity occurring in the detection wavelength band of the first emission signal and intensity occurring in the detection wavelength band of the other emission signal in a test situation where only the analyte causing the first emission signal is present.
  • the measured intensity of the first emission signal may be at least partially caused by a background signal that is present also when the first emission signal is not generated in detection reactions.
  • the contribution of the background signal should be sufficiently eliminated from the measured intensity of the first emission signal prior to the cross-talk correction.
  • the contribution of the background signal and the cross-talk parameter can be determined on the basis of intensities measured from appropriate test samples. In many cases the situation is, however, more complicated so that none of the emission signals can be measured cross-talk free, i.e. the emission signals are spectrally and temporally so overlapping that it is not possible to select such temporal detection windows and/or detection wavelength bands so that at least one of the emission signals could be measured cross-talk free.
  • each FRET-probe comprises a donor, an acceptor, and a reactive region capable of specifically hybridizing with its complementary target sequence, i.e.
  • the time-resolved fluorescence emission signal of a population of probes of a given type comprises two signal components: a first signal component belonging to the acceptors excited due to the energy transfer from the excited donors and a second signal component belonging to the excited donors which do not participate to the energy transfer.
  • the acceptor is preferably selected so that its emission spectrum has a maximum at a wavelength where the donor has a local minimum in its emission spectrum.
  • the decay time of the energy transfer induced acceptor emission is dependent on the energy transfer efficiency, which in turn is inversely proportional to distance between the acceptor and the donor.
  • Decay time of energy transfer induced acceptor emission is significantly faster when the probes are unhybridized, i.e. a short donor-acceptor distance, than when the probes are hybridized with the target analyte, i.e. a longer donor-acceptor distance.
  • acceptor emission signal of hybridized probes can be separated from acceptor emission signal of unhybridized probes using a suitable temporal detection window.
  • Acceptor emission signals of different probes hybridized with different target analytes can be separated from each other by using appropriate detection wavelength bands but, as mentioned above, the cross-talk complicates the situation. The situation is further complicated by the fact that the background emission caused by excited donors that do not participate to the energy transfer is dependent on the percentage of hybridized probes from all probes in a sample under consideration.
  • each detection wavelength band relates to one of analyte-specific probe-populations contained by the sample, and each probe-population is, after excitation, capable of emitting a first signal component and a second signal component whose spectra are mutually different and at least the first signal component is dependent on presence of analyte detectable with that probe-population.
  • sample means substance that comprises one or more analytes to be detected and assay reagents needed for the detection, said assay reagents containing the above-mentioned probe-populations.
  • the method comprises: - computing estimates of cross-talk intensities occurring on the detection wavelength bands and at least partially caused by the second signal components emitted by the probe-populations on the basis of: a) first cross-talk parameters and b) at least one value indicative of at least one intensity occurring on at least one auxiliary wavelength band outside the detection wavelength bands and at least partially caused by the second signal components, and
  • each of the first cross-talk parameters indicates a relation between a) intensity occurring on one of the detection wavelength bands and at least partially caused by the second signal components, and b) intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components, and
  • each of the second cross-talk parameters indicates a relation between a) intensity occurring on the detection wavelength band related to one of the probe-populations and at least partially caused by the first signal component emitted by another of the probe-populations, and b) intensity occurring on the detection wavelength band related to the other of the probe-populations and at least partially caused by the first signal component emitted by the other of the probe-populations.
  • the probe-populations can be, for example but not necessarily, populations of probes based on the fluorescence resonance energy transfer "FRET".
  • the method for cross-talk correction can be used, for example, in conjunction with time- resolved fluorescence resonance energy transfer "TR-FRET" based multianalyte detections that are suitable for e.g. Severe Combined Immunodeficiency "SCID" assays.
  • the value indicative of the intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components has a value measured from the sample on the auxiliary wavelength band.
  • the dependency of the background emission on the percentage of hybridized probes from all probes can be taken into account in the cross-talk correction.
  • the intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components is preferably measured from each sample well separately.
  • a device for cross-talk correction of intensities measured on two or more detection wavelength bands from a sample to be analyzed comprises a computing system configured to:
  • each of the second cross-talk parameters indicates a relation between a) intensity occurring on the detection wavelength band related to one of the probe-populations and at least partially caused by the first signal component emitted by another of the probe-populations, and b) intensity occurring on the detection wavelength band related to the other of the probe-populations and at least partially caused by the first signal component emitted by the other of the probe-populations.
  • an instrument comprising:
  • a computer program for for cross-talk correction of intensities measured on two or more detection wave- length bands from a sample to be analyzed.
  • the computer program comprises computer executable instructions for controlling a programmable processor to:
  • each of the first cross-talk parameters indicates a relation between a) intensity occurring on one of the detection wavelength bands and at least partially caused by the second signal components, and b) intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components, and
  • each of the second cross-talk parameters indicates a relation between a) in- tensity occurring on the detection wavelength band related to one of the probe-populations and at least partially caused by the first signal component emitted by another of the probe-populations, and b) intensity occurring on the detection wavelength band related to the other of the probe-populations and at least partially caused by the first signal component emitted by the other of the probe-populations.
  • a computer program product according to the disclosure comprises a non-volatile computer readable medium, e.g. a compact disc ("CD”), encoded with a computer program according to the disclosure.
  • a non-volatile computer readable medium e.g. a compact disc (“CD")
  • figure 1 shows a flow chart of a method according to an exemplifying embodiment for cross-talk correction of intensities measured on two or more detection wavelength bands from a sample to be analyzed
  • figure 2 illustrates emission spectra of two probe-populations in an exemplifying case where a method according to an exemplifying embodiment for cross-talk cor- rection is applicable
  • figure 3a shows a schematic illustration of an optical measurement instrument comprising a device according to an exemplifying embodiment for cross-talk correction of intensities measured on two or more detection wavelength bands from a sample to be analyzed
  • figure 3b shows schematic illustration of a view seen downwards from the line A-A of figure 3a.
  • Figure 1 shows a flow chart of a method according to an exemplifying embodiment for cross-talk correction of intensities measured, from a sample to be analyzed, on mutually non-overlapping detection wavelength bands.
  • Each of the detection wavelength bands relates to one of analyte-specific probe-populations contained by the sample.
  • An emission signal of each probe-population contains a first signal component whose spectrum has a maximum at a wavelength specific to that probe-population and which is dependent on concentration of analyte detectable with that probe-population and a second signal component whose spectrum is different from the spectrum of the above-mentioned first signal component.
  • Figure 2 illustrates emission spectra in an exemplifying case where there are probe- populations Pi and P 2 .
  • a solid line 213 provided with circles represents the aggregate, i.e. the sum, of the emission spectra of the probe-populations Pi and P 2 .
  • the aggregate of the emission spectra represents the spectrum of the signal that can be measured from the sample when using a certain excitation wavelength.
  • a solid line 201 represents the spectrum of the first signal component emitted by the probe-population P-i
  • a solid line 202 represents the spectrum of the second signal component emitted by the probe-population P-i.
  • a dashed line 21 1 represents the spectrum of the first signal component emitted by the probe-population P 2 and a dashed line 212 represents the spectrum of the second signal component emitted by the probe-population P 2 .
  • a wavelength band 220 shown in figure 2 represents the detection wavelength band related to the probe-population P-i
  • a wavelength band 221 represents the detection wavelength band related to the probe-population P 2 .
  • the probe-populations Pi and P 2 can be, for example but not necessarily, populations, i.e. groups, of probes based on fluorescence resonance energy transfer "FRET" where each probe may comprise at least one donor, at least one acceptor, and at least one reactive region capable of interacting with the analyte to be detected with that probe.
  • the donor and the acceptor of a probe can be attached to a same molecule but it is also possible that a probe comprises a donor attached to a first molecule and an acceptor attached to a second, separate, molecule. In this case, the mutually separate donor and acceptor can interact with the analyte to be detected and thereby form a donor-acceptor pair suitable for e.g. the fluorescence resonance energy transfer "FRET".
  • the donor can be a luminescent label having luminescent lifetime longer than e.g. 1 ⁇ .
  • Each of the probes may comprise, for example, a lanthanide chelate donor and an organic fluorophore acceptor.
  • the lanthanide can be, for example, europium "Eu”, terbium “Tb”, dysprosium “Dy”, or samarium “Sm”.
  • the acceptor of the probe-population Pi can be, for example, Alexa Fluor® 647 dye and the acceptor of the probe-population P 2 can be, for example, Alexa Fluor® 750 dye.
  • ⁇ 0 , ⁇ - ⁇ , and ⁇ 2 shown in figure 2 would be ⁇ 0 s 615 nm, ⁇ « 665 nm, and ⁇ 2 « 780 nm, where ⁇ 0 is the center point of a 610-620 nm auxiliary wavelength band 230 shown in figure 2, ⁇ is the center point of the 660-670 nm detection wavelength band 220, and ⁇ 2 is the center point of the 775-785 nm detection wavelength band 221 .
  • the spectrum depicted with the solid line 201 is caused by the Alexa Fluor® 647 acceptors of the probes of the probe-population Pi excited due to the energy transfer from the excited Eu donors of these probes, and the spectrum depicted with the solid line 202 is caused by the excited Eu donors of the probes of the probe-population P not participating to the energy transfer.
  • the spectrum depicted with the dashed line 21 1 is caused by the Alexa Fluor® 750 acceptors of the probes of the probe-population P 2 excited due to the energy transfer from the excited Eu donors of the probes of the probe-population P 2
  • the spectrum depicted with the dashed line 21 2 is caused by the excited Eu donors of the probes of the probe- population P 2 not participating to the energy transfer.
  • Figure 2 can be deemed to represent a time instant after donor excitation when signals emitted by acceptors of unhybridized, i.e. free, probes have already been decayed off sufficiently from the viewpoint of detection.
  • a method according to an exemplifying embodiment for cross-talk correction of intensities I MI and IM2 measured on the detection wavelength bands 220 and 221 , respectively, comprises the following actions:
  • figure 1 computing estimates of cross-talk intensities C B i and C B 2 occurring on the detection wavelength bands 220 and 221 and at least partially caused by the second signal components emitted by the probe-populations Pi and P 2 on the basis of : a) first cross-talk parameters R B i and R B2 and b) a value l BM indicative of intensity at least partially caused by the second signal components and occurring on the auxiliary wavelength band 230, figure 2, outside the detection wavelength bands 220 and 221 , and
  • figure 1 computing cross-talk corrected intensities l C i and l C 2 of the detection wavelength bands 220 and 221 on the basis of: a) the intensities IMI and I M2 measured on the detection wavelength bands 220 and 221 , b) the computed estimates of the cross-talk intensities C B i and C B2 , and c) second cross-talk parameters R-
  • the above-mentioned cross-talk intensities CBI and C B2 can be called “background” intensities so as to be coherent with phraseology related to TR-FRET.
  • the cross-talk parameter R B i indicates a relation between a) intensity occurring on the detection wavelength band 220 and at least partially caused by the second signal components emitted by the probe-populations Pi and P 2 , and b) intensity occurring on the auxiliary wavelength band 230 and at least partially caused by the second signal components.
  • the cross-talk parameter R B 2 indicates a relation between a) intensity occurring on the detection wavelength band 221 and at least partially caused by the second signal components, and b) intensity occurring on the auxiliary wavelength band 230 and at least partially caused by the second signal components.
  • the spectra of the second signal components emitted by different probe-populations are different from each other, e.g. the spectrum of the second signal component of the probe-population P can be different from that of the second signal component of the probe-population P 2 .
  • the cross-talk parameter Ri 2 indicates a relation between a) intensity occurring on the detection wavelength band 220 and at least partially caused by the first signal component emitted by the probe-population P 2 , and b) intensity occurring on the detection wavelength band 221 and at least partially caused by the first signal component emitted by the probe-population P 2 .
  • the cross-talk parameter R 2 i indicates a relation between a) intensity occurring on the detection wavelength band 221 and at least partially caused by the first signal component emitted by the probe-population P ; and b) intensity occurring on the detection wavelength band 220 and at least partially caused by the first signal component emitted by the probe-population P-i .
  • the value I B M indicative of the intensity occurring on the auxiliary wavelength band 230 and at least partially caused by the second signal components of the probe-populations Pi and P 2 is a value measured on the auxiliary wavelength band from the sample to be analyzed. Therefore, for example in conjunction with FRET-based assays where the intensity of signal caused by the second signal components is at least partially dependent on the concentrations of the analytes present in the sample, the IBM can be measured and taken into account in the cross-talk correction from each sample well separately.
  • the value IBM indicative of the intensity occurring on the auxiliary wavelength band 230 and at least partially caused by the second signal components is a same pre- determined value in conjunction with several samples, e.g. a same value IBM can be used for many sample wells.
  • the estimates of the crosstalk intensities CBI and CB2 are computed according to the following equation:
  • the cross-talk corrected intensities Id and Ic2 of the detection wavelength bands 220 and 221 are solved from the following pair of equations:
  • the cross-talk corrected intensities of the detection wavelength bands can be solved from the following set of equations:
  • n is the number of the analyte-specific probe-populations
  • lci and lq are the cross-talk corrected intensities of the i th and j th ones of the detection wavelength bands, respectively
  • I MI is the intensity measured on the i th one of the detection wavelength bands
  • Cej is the estimate of the cross-talk intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the second signal components
  • R is the second cross-talk parameter that indicates a ratio between a) intensity occurring on the i th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands and b) intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands.
  • a method according to an exemplifying embodiment comprises determining the first cross-talk parameters on the basis of first test intensities measured from one or more first model samples each of which contains one or more of the probe- populations and is free from analytes detectable with the probe-populations.
  • the first cross-talk parameters can be computed, for example, according to the equation:
  • i 1 , 2, the number of the analyte-specific probe-populations
  • RB I is the first cross-talk parameter related to the i th one of the detection wavelength bands, e.g. one of the wavelength bands 220 and 221 shown in figure 2
  • l M odeio,i is the first test intensity occurring on i th one of the detection wavelength bands and at least partially caused by the second signal components and measured from such a first model sample that contains the probe-populations
  • iModeio.B is the first test intensity occurring on the auxiliary wavelength band, e.g. the wavelength band 230 shown in figure 2, and at least partially caused by the second signal components and measured from the first model sample.
  • a method comprises determining the second cross-talk parameters on the basis of second test intensities measured from second model samples, where each of the second model samples contains one or more of the probe-populations and analyte detectable with one of the probe-populations and is free from analytes detectable with the other probe- populations.
  • R is the second cross-talk parameter related to the i th and j th ones of the detec- tion wavelength bands, e.g. the wavelength bands 220 and 221 shown in figure 2,
  • i Modei, ij is the second test intensity occurring on the i th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands and measured from a such second model sample that contains analyte detectable with the probe-population related to the j th one of the detection wavelength bands and is free from analytes detectable with the other probe-populations,
  • IModei, jj is the second test intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands and measured from the above-mentioned second model sample, and
  • Ci and Cj are real valued adjustment terms.
  • C is test intensity I Modeio occurring on i th one of the detection wavelength bands and at least partially caused by the second signal components
  • Cj is test intensity IModeio occurring on j th one of the detection wavelength bands and at least partially caused by the second signal components
  • the real valued adjustment terms C, and C j 0.
  • the first and second crosstalk parameters are selected from among pre-determined values on the basis of at least one of the following: ways of conduct of intensity measurements, information identifying a measurement instrument used for the intensity measurements.
  • a way of conduct of intensity measurement can be characterized by, for example but not necessarily, the number of successive excitation-counting cycles used in detection of intensity on a certain measurement wavelength band, where each excitation- counting cycle contains an excitation phase and a subsequent counting phase.
  • the information identifying a measurement instrument can be, for example, a serial number of the measurement instrument used for the intensity measurements.
  • a computer program according to an exemplifying embodiment comprises computer executable instructions for controlling a programmable processor to carry out a method according to any of the above-described exemplifying embodiments.
  • the computer executable instructions can be generated with a suitable programming language.
  • a computer program product according to an exemplifying embodiment comprises a non-volatile computer readable medium, e.g. a compact disc ("CD"), encoded with a computer program according to an embodiment.
  • CD compact disc
  • a signal according to an exemplifying embodiment is encoded to carry information defining a computer program according to an embodiment.
  • Figure 3a shows a schematic illustration of an optical measurement instrument that comprises a device according to an exemplifying embodiment for cross-talk correction of intensities measured on two or more wavelength bands from a sample to be analyzed.
  • Figure 3b shows schematic illustration of a view seen downwards from the line A-A of figure 3a.
  • the measurement instrument comprises me- chanical support elements arranged to support a sample plate 308 that can be e.g. a microtitration plate.
  • the sample plate comprises sample wells which contain samples 351 , 352, 353, 354, 355, 356, and 357 to be analyzed.
  • the samples have been arranged to comprise analyte-specific probe-populations, e.g. FRET-probes, in order to detect presence of two or more analytes from each sample.
  • the me- chanical support elements comprise a support rail 306 and guide elements 309 shown in figure 3b.
  • the support rail 306 is supported relative to a body of the measurement instrument with the aid of the guide elements 309 in such a way that the support rail 306 is movable in the directions of a two-headed arrow 310 shown in figure 3b.
  • the mechanical support elements comprise a sledge 307 capable of receiving the sample plate 308.
  • the sledge is connected to the support rail 306 in such a way that the sledge is capable of sliding along the support rail in the longitudinal direction of the support rail, i.e. the sledge is movable with respect to the support rail 306 in the directions of a two-headed arrow 31 1 shown in figure 3b.
  • the sample plate 308 is movable in the xy-plane defined by a co-ordinate system 390. Due to the fact that the sample wells are movable in the xy-plane, the contents of different sample wells can be measured in a temporally successive manner so that each sample well is in turn the sample well whose content is being measured.
  • the measurement instrument comprises measurement equipment for measuring intensities on two or more detection wavelength bands from a sample to be analyzed.
  • Each detection wavelength band relates to one of analyte-specific probe- populations contained by the sample, and each probe-population is, after excitation, capable of emitting at least a first signal component and a second signal component whose spectra have maxima at different wavelengths and at least the first signal component is dependent on presence of analyte detectable with that probe-population.
  • the measurement equipment comprises an excitation light source 303, figure 3a, and a light guide 304 for directing excitation radiation to the sample 352 being measured.
  • the measurement equipment comprises a detector 302 for measuring, on appropriate wavelength bands, the emission radiation emit- ted by the sample 352 and for producing a signal indicative of intensities of the emission radiation measured on the wavelength bands.
  • the detector 309 can be based on, for example, a photodiode or a photomultiplier tube.
  • the measurement instrument comprises a controller 301 for controlling the operation of the excitation light source 303 and the detector 302.
  • the excitation light source 303, the detector 302, and/or the light guide 304 can be either integral or replaceable components of the measurement instrument.
  • the controller 301 can be can be implemented with one or more programmable processor circuits, one or more dedicated hardware circuits such as an application specific integrated circuit "ASIC", one or more field programmable logic circuits such as a field programmable gate array "FPGA”, or a combination of these.
  • the optical measurement instrument may comprise an optical filtering device with the aid of which an appropriate wave- length band can be selected for each measurement.
  • the measurement instrument comprises a device for cross-talk correction of the intensities measured on the two or more detection wavelength bands from the sample 352.
  • the device comprises:
  • the controller 301 comprises a computing system that is configured to constitute the device for cross- talk correction.
  • the device for cross-talk correction is implemented with a separate computing system.
  • the computing system is configured to compute the estimates of the cross-talk intensities occurring on the detection wavelength bands and at least partially caused by the second signal components according to the following equation : where CBI is the estimate of the cross-talk intensity occurring on the i th one of the detection wavelength bands and at least partially caused by the second signal components, R B i is the first cross-talk parameter related to the i th one of the detection wavelength bands, and I BM is the value indicative of the intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components.
  • the computing system is configured to solve the cross-talk corrected intensities of the detection wavelength bands from the following set of equations: where:
  • I ci and lq are the cross-talk corrected intensities of the i th and j th ones of the detection wavelength bands, respectively, I MI is the intensity measured on the i th one of the detection wavelength bands,
  • C B j is the estimate of the cross-talk intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the second signal components
  • R is the second cross-talk parameter that indicates a ratio between a) intensity occurring on the i th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands and b) intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands.
  • the computing system is configured determine the first cross-talk parameters on the basis of first test intensities measured from one or more first model samples each of which contains one or more of the probe-populations and is free from analytes detectable with the probe-populations.
  • the computing system is configured to compute the first cross-talk parameters according to the equation : p _ ⁇ ModelO, i
  • R B i is the first cross-talk parameter related to the i th one of the detection wavelength bands
  • iModeio.i is the first test intensity occurring on i th one of the detection wavelength bands and at least partially caused by the second signal components and measured from such a first model sample that contains the probe-populations
  • iModeio.B is the first test intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components and measured from the first model sample.
  • the computing system is configured determine the second cross-talk parameters on the basis of second test intensities measured from second model samples, where each of the second model samples contains one or more of the probe-populations and analyte detectable with one of the probe-populations and is free from analytes detectable with the other probe-populations.
  • the computing system is configured to compute the second cross-talk parameters according to the equa- tion: p I
  • R is the second cross-talk parameter related to the i th and j th ones of the detection wavelength bands
  • I Model, i,j is the second test intensity occurring on the i th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wavelength bands and measured from the second model sample that contains analyte detectable with the probe-population related to the j th one of the detection wavelength bands and is free from analytes detectable with the other probe-populations,
  • I Model, j,j is the second test intensity occurring on the j th one of the detection wavelength bands and at least partially caused by the first signal component emitted by the probe-population related to the j th one of the detection wave- length bands and measured from the second model sample, and
  • Ci and Cj are real valued adjustment terms.
  • the computing system is configured to set the adjustment terms so that C, is test intensity occurring on i th one of the detection wavelength bands and at least partially caused by the second signal components, and Cj is test intensity occurring on j th one of the detection wavelength bands and at least partially caused by the second signal components, where the test intensities C, and Cj are measured from a model sample that contains the probe-populations and is free from analytes detectable with the probe- populations.
  • the measurement equipment is configured to measure the intensity occurring on the auxiliary wavelength band and at least partially caused by the second signal components from the sample 352, and the device for cross-talk correction is config- ured to use the measured intensity when computing the estimates of the cross-talk intensities occurring on the detection wavelength bands and at least partially caused by the second signal components.
  • the device for cross-talk correction is configured to select the first and second cross-talk parameters from among pre-determined values on the basis of at least one of the following: ways of conduct of intensity measurements, information identifying the measurement instrument from among similar measurement instruments.
  • the information identifying a measurement instrument can be, for example, a serial number of the measurement instrument.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Immunology (AREA)
  • Zoology (AREA)
  • General Physics & Mathematics (AREA)
  • Wood Science & Technology (AREA)
  • Pathology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Computer Networks & Wireless Communication (AREA)
  • Theoretical Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Mathematical Physics (AREA)
  • Molecular Biology (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
PCT/FI2014/050246 2013-04-15 2014-04-08 A method and a device for cross-talk correction of measured intensities WO2014170537A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US14/784,768 US9736555B2 (en) 2013-04-15 2014-04-08 Method and a device for cross-talk correction of measured intensities
BR112015025832-8A BR112015025832B1 (pt) 2013-04-15 2014-04-08 Método e dispositivo para correção de diafonia e instrumento de medida
CN201480033905.7A CN105324493B (zh) 2013-04-15 2014-04-08 用于测量强度的串扰校准的方法和设备
EP14721911.7A EP2986737A1 (en) 2013-04-15 2014-04-08 A method and a device for cross-talk correction of measured intensities

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201361811847P 2013-04-15 2013-04-15
US61/811,847 2013-04-15
FI20135367 2013-04-15
FI20135367 2013-04-15

Publications (1)

Publication Number Publication Date
WO2014170537A1 true WO2014170537A1 (en) 2014-10-23

Family

ID=51730861

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FI2014/050246 WO2014170537A1 (en) 2013-04-15 2014-04-08 A method and a device for cross-talk correction of measured intensities

Country Status (6)

Country Link
US (1) US9736555B2 (pt)
EP (1) EP2986737A1 (pt)
CN (1) CN105324493B (pt)
BR (1) BR112015025832B1 (pt)
TW (1) TWI611174B (pt)
WO (1) WO2014170537A1 (pt)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050123957A1 (en) * 2003-10-01 2005-06-09 Wallac Oy Homogeneous time-resolved energy transfer assay
US20060147954A1 (en) 2004-10-19 2006-07-06 Wallac Oy Novel probe and its use in bioaffinity assays
US20110301062A1 (en) * 2008-06-11 2011-12-08 Jiang Zhu Reliable fluorescence correction method for two-color measurement fluorescence system

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI963989A (fi) 1996-10-04 1998-04-05 Wallac Oy Homogeenisiä määritysmenetelmiä, jotka perustuvat luminesenssienergiasiirtoon
US7209836B1 (en) 1999-07-16 2007-04-24 Perkinelmer Las, Inc. Method and system for automatically creating crosstalk-corrected data of a microarray
AU2002308693A1 (en) 2001-04-25 2002-11-05 Amnis Corporation Method and apparatus for correcting crosstalk and spatial resolution for multichannel imaging
EP1288308A1 (en) 2001-08-28 2003-03-05 Roche Diagnostics GmbH A method for the determination of multiple analytes
FI20095302A0 (fi) * 2009-03-24 2009-03-24 Arctic Partners Oy Ab Luminesenssimääritysmenetelmä
US8435738B2 (en) * 2011-09-25 2013-05-07 Theranos, Inc. Systems and methods for multi-analysis

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050123957A1 (en) * 2003-10-01 2005-06-09 Wallac Oy Homogeneous time-resolved energy transfer assay
US20060147954A1 (en) 2004-10-19 2006-07-06 Wallac Oy Novel probe and its use in bioaffinity assays
US20110301062A1 (en) * 2008-06-11 2011-12-08 Jiang Zhu Reliable fluorescence correction method for two-color measurement fluorescence system

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
ELDER A D ET AL: "A quantitative protocol for dynamic measurements of protein interactions by Forster resonance energy transfer-sensitized fluorescence emission", JOURNAL OF THE ROYAL SOCIETY. INTERFACE, THE ROYAL SOCIETY, LONDON, GB, vol. 6, no. Suppl. 1, 2009, pages S59 - S81, XP009168413, ISSN: 1742-5689, [retrieved on 20090206], DOI: 10.1098/RSIF.2008.0381.FOCUS *
MASILAMANI ELANGOVAN ET AL: "Characterization of one- and two-photon excitation fluorescence resonance energy transfer microscopy", METHODS, vol. 29, no. 1, 2003, pages 58 - 73, XP055121552, ISSN: 1046-2023, DOI: 10.1016/S1046-2023(02)00283-9 *
TAKANISHI C L ET AL: "GFP-based FRET analysis in live cells", BRAIN RESEARCH, ELSEVIER, AMSTERDAM, NL, vol. 1091, no. 1, 26 May 2006 (2006-05-26), pages 132 - 139, XP027917893, ISSN: 0006-8993, [retrieved on 20060526] *
V. LAITALA ET AL.: "Time-resolved detection probe for homogeneous nucleic acid analyses in one-step format", ANALYTICAL BIOCHEMISTRY, vol. 361, 2007, pages 126 - 131, XP005733813, DOI: doi:10.1016/j.ab.2006.11.015
YE CHEN ET AL: "Quantitative FRET data analysis: protein localization in living specimens", PROCEEDINGS OF SPIE, vol. 6089, 9 February 2006 (2006-02-09), pages 60891W - 60891W-9, XP055121557, ISSN: 0277-786X, DOI: 10.1117/12.658170 *

Also Published As

Publication number Publication date
US20160066072A1 (en) 2016-03-03
BR112015025832B1 (pt) 2022-03-15
TW201447275A (zh) 2014-12-16
BR112015025832A2 (pt) 2017-07-25
EP2986737A1 (en) 2016-02-24
CN105324493B (zh) 2018-02-23
TWI611174B (zh) 2018-01-11
US9736555B2 (en) 2017-08-15
BR112015025832A8 (pt) 2019-12-24
CN105324493A (zh) 2016-02-10

Similar Documents

Publication Publication Date Title
Zhou et al. Design principles of spectroscopic probes for biological applications
US8625100B2 (en) Method for the optical determining of a measured variable of a medium
JP7038158B2 (ja) 蛍光検出のための方法およびシステム
US8729502B1 (en) Simultaneous, single-detector fluorescence detection of multiple analytes with frequency-specific lock-in detection
Sutariya et al. A unique fluorescence biosensor for selective detection of tryptophan and histidine
CN101788479A (zh) 对基于量子点的荧光共振能量转移进行高灵敏度检测的方法
Hoffmann et al. Nanoparticle-encapsulated vis-and NIR-emissive fluorophores with different fluorescence decay kinetics for lifetime multiplexing
JP2010511148A (ja) 生物検定における分子の多変検出
JP2009250721A (ja) 分子間相互作用の解析方法
JP2005513497A (ja) 試料担体上および/または試料担体中の蛍光性、ルミネセンス発光性および/または吸光性物質の同定のための方法および/または装置
US20040023229A1 (en) Direct detection of individual molecules
JPWO2004090517A1 (ja) 蛍光寿命を利用した物質の定量用試薬、方法及び装置
Sutariya et al. A pyrenyl linked calix [4] arene fluorescence probe for recognition of ferric and phosphate ions
US20220196561A1 (en) Optical sensor element, optical ph sensor and method for monitoring the function of an optical ph sensor
US9736555B2 (en) Method and a device for cross-talk correction of measured intensities
CN1142423C (zh) 定量测量荧光共振能量转移效率的方法
US20200003765A1 (en) Method and apparatus for detecting an analyte
US11971354B2 (en) Methods and systems for fluorescence detection using infrared dyes
Ma et al. Time-resolved fluorescence assays
US20060115842A1 (en) Highly sensitive homogeneous assay based on anti-Stokes' shift FRET measurement
Prakash et al. White light excitation fluorescence (WLEF) Part II. Analysis of complex multifluorophoric systems
JP5208774B2 (ja) 蛍光分光光度計
Gutmann et al. UV fluorescence detection and spectroscopy in chemistry and life sciences
EP3161456B1 (en) A device and a method for detecting a sample contained by a sample well
KR102077775B1 (ko) 형광시정수를 이용한 체외 진단방법 및 이를 위한 체외 진단시스템

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201480033905.7

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14721911

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 14784768

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 2014721911

Country of ref document: EP

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112015025832

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112015025832

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20151009